Inorganic solids are a kind of important catalysts, and their activities usually come from sparse active sites, which are structurally different from inactive bulk. Therefore, the rational optimization of activity depends on studying these active sites. Copper is a widely used catalyst and is expected to be a promising catalyst for the electroreduction of CO to CH. Here, we report a conductive dinuclear cuprous complex with a short Cu···Cu contact for the electroreduction of CO to CH. By using 1-[1,10]phenanthrolin-2-one and Cu(I) ions, a dinuclear cuprous complex [Cu(ophen)] (Cuophen) with a remarkable conductivity (3.9 × 10 S m) and a short intramolecular Cu···Cu contact (2.62 Å) was obtained. Such a short Cu···Cu contact is close to the distance of 2.54 Å between 2 adjacent Cu atoms in the edge of the copper(100)/(111) plane. Detailed examination of Cuophen revealed a high activity for the electroreduction of CO to CH with a Faradaic efficiency of 55(1)% and a current density of 580 mA cm, and no obvious degradation was observed over 50 h of continuous operation. Comparing the properties and mechanisms of Cuophen and 2 other copper complexes with different Cu···Cu distances, we found that the shorter Cu···Cu distance is conducive not only for a *CO species to bridge 2 copper ions into a more stable intermediate transition state but also for C-C coupling.
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http://dx.doi.org/10.34133/research.0008 | DOI Listing |
Inorg Chem
July 2023
Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry, School of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, People's Republic of China.
The unraveling of the stimuli-responsive mechanism is crucial to the design and precise synthesis of stimuli-responsive luminescent materials. We report herein the mechanochromic and selective vapochromic solid-state luminescence properties of a new bimetallic cuprous complex [{Cu(bpmtzH)}(μ-dppm)](ClO) (), and the corresponding response mechanisms are elucidated by investigating its two different solvated polymorphs ·2CHCl () and ·2CHCl (). Green-emissive and cyan-emissive can be interconverted upon alternate exposure to CHCl and CHCl vapors, which is principally attributable to a combined alteration of both intermolecular NH···OClO hydrogen bonds and intramolecular "triazolyl/phenyl" π···π interactions induced by different solvents.
View Article and Find Full Text PDFResearch (Wash D C)
December 2022
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.
Inorganic solids are a kind of important catalysts, and their activities usually come from sparse active sites, which are structurally different from inactive bulk. Therefore, the rational optimization of activity depends on studying these active sites. Copper is a widely used catalyst and is expected to be a promising catalyst for the electroreduction of CO to CH.
View Article and Find Full Text PDFInorg Chem
October 2022
Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry, School of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, People's Republic of China.
A thermo-, mechano-, and vapochromic bimetallic cuprous-emissive complex has been reported, and the origin and application of its tri-stimuli-responsive luminescence have been explored. As revealed by single-crystal structure analysis, thermo- and vapochromic luminescence adjusted by heating at 60 °C and CHCN vapor fuming, accompanied by a crystalline-to-crystalline transition, is due to the breaking and rebuilding of the CHCN-Cu bond, as supported by H nuclear magnetic resonance (NMR), Fourier-transform infrared (FT-IR) spectroscopy, powder X-ray diffraction (PXRD), thermogravimetry (TG), and time-dependent density functional theory (TD-DFT) analyses of the CHCN-coordinated species [Cu(μ-dppa)(μ-η(N)η(N,N)-fptz)(CHCN)](ClO)·HO () and its CHCN-removed derivative [Cu(μ-dppa)(μ-η(N)η(N,N)-fptz)](ClO)·HO (). Luminescence mechanochromism, mixed with a crystalline-to-amorphous transition where the initial crystalline is different for and , is mainly assigned as the destruction of the CHCN-Cu bonding and/or the O···HN and OH···N hydrogen bonds.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2022
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, China.
Cu-based metal-organic frameworks have attracted much attention for electrocatalytic CO reduction, but they are generally instable and difficult to control the product selectivity. We report flexible Cu(I) triazolate frameworks as efficient, stable, and tunable electrocatalysts for CO reduction to C H /CH . By changing the size of ligand side groups, the C H /CH selectivity ratio can be gradually tuned and inversed from 11.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2020
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
After a general introduction to the features and mechanisms of cytochrome c oxidases (CcOs) in mitochondria and aerobic bacteria, we present DFT calculated physical and spectroscopic properties for the catalytic reaction cycle compared with experimental observations in bacterial ba3 type CcO, also with comparisons/contrasts to aa3 type CcOs. The Dinuclear Complex (DNC) is the active catalytic reaction center, containing a heme a3 Fe center and a near lying Cu center (called CuB) where by successive reduction and protonation, molecular O2 is transformed to two H2O molecules, and protons are pumped from an inner region across the membrane to an outer region by transit through the CcO integral membrane protein. Structures, energies and vibrational frequencies for Fe-O and O-O modes are calculated by DFT over the catalytic cycle.
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